Technology Process of C45H39ClFN5O5
There total 6 articles about C45H39ClFN5O5 which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
2,3,5-trimethyl-pyridine; silver nitrate;
In
dichloromethane;
at 20 ℃;
for 12h;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sulfuric acid / acetic acid / 12 h / 0 - 20 °C
2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.5 h / 0 - 20 °C / Inert atmosphere
2.2: 4 h / 0 - 60 °C
3.1: silver nitrate; 2,3,5-trimethyl-pyridine / dichloromethane / 12 h / 20 °C
With
2,3,5-trimethyl-pyridine; sulfuric acid; silver nitrate; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
dichloromethane; acetic acid; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / acetonitrile / 12 h / 80 °C
2.1: tetrahydrofuran / 12 h / -78 - 20 °C / Inert atmosphere
3.1: dmap; triethylamine / dichloromethane / 12 h / 20 °C / Cooling with ice
4.1: sulfuric acid / acetic acid / 12 h / 0 - 20 °C
5.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.5 h / 0 - 20 °C / Inert atmosphere
5.2: 4 h / 0 - 60 °C
6.1: silver nitrate; 2,3,5-trimethyl-pyridine / dichloromethane / 12 h / 20 °C
With
2,3,5-trimethyl-pyridine; dmap; sulfuric acid; silver nitrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; dichloromethane; acetic acid; acetonitrile;